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首页> 外文期刊>The Journal of molecular diagnostics: JMD >Diagnosis of hydatidiform moles by polymorphic deletion probe fluorescence in situ hybridization.
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Diagnosis of hydatidiform moles by polymorphic deletion probe fluorescence in situ hybridization.

机译:通过多态性缺失探针荧光原位杂交诊断葡萄胎。

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Because products of conception often contain maternal and villous tissues, the determination of maternal and villous genotypes based on genetic polymorphisms can help discern maternal and paternal chromosomal contribution and aid in the diagnosis of hydatidiform moles. Polymorphic deletion probe (PDP) fluorescence in situ hybridization (FISH) probes based on copy number variants are highly polymorphic and allow in situ determination of genetic identity. By using three informative PDPs on chromosomes 2p, 4q, and 8p, we compared maternal with villous genotypes and determined the ploidy of villous tissue. PDP FISH was performed on 13 complete moles, 13 partial moles, 13 nonmolar abortions, and an equivocal hydropic abortion. PDP FISH permitted definitive diagnosis of complete moles in five of 13 cases for which maternal and villous genotypes were mutually exclusive. A complete mole was highly suspected when all three PDP loci showed homozygous villous genotypes. The diagnosis of a complete mole by PDP FISH yielded a theoretical test sensitivity of 87.5%, specificity of 91.8%, an observed test sensitivity of 100%, and specificity of 92.3%. Triploidy was observed in all partial moles, in which diandric triploidy was confirmed in six cases. In the equivocal hydropic abortion, PDP FISH combined with p57 immunofluorescence revealed placental androgenetic/biparental mosaicism. PDP FISH can be used in clinical practice and research studies to subclassify hydatidiform moles and evaluate unusual products of conception.
机译:由于受孕产物通常包含母体和绒毛组织,因此基于遗传多态性确定母体和绒毛基因型可以帮助辨别母体和父体的染色体贡献,并有助于葡萄胎的诊断。基于拷贝数变异的多态性缺失探针(PDP)荧光原位杂交(FISH)探针具有高度多态性,可以原位确定遗传同一性。通过在染色体2p,4q和8p上使用三个信息丰富的PDP,我们比较了母体和绒毛基因型,并确定了绒毛组织的倍性。 PDP FISH在13个完全痣,13个部分痣,13个非摩尔流产和模棱两可的水镜流产上进行。 PDP FISH在母体和绒毛基因型互斥的13例病例中有5例可以明确诊断完整的痣。当所有三个PDP基因座均显示纯合的绒毛基因型时,高度怀疑有完整的痣。通过PDP FISH诊断完全葡萄胎的理论测试灵敏度为87.5%,特异性为91.8%,观察到的测试灵敏度为100%,特异性为92.3%。在所有部分葡萄胎中均观察到三倍体,其中六例证实为双三倍体。在模棱两可的流产中,PDP FISH结合p57免疫荧光显示胎盘雄激素/双亲镶嵌。 PDP FISH可用于临床实践和研究研究,以对葡萄胎进行细分,并评估异常的受孕产物。

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